CN105814092B - 亲水性固化物用组合物 - Google Patents
亲水性固化物用组合物 Download PDFInfo
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- CN105814092B CN105814092B CN201480067496.2A CN201480067496A CN105814092B CN 105814092 B CN105814092 B CN 105814092B CN 201480067496 A CN201480067496 A CN 201480067496A CN 105814092 B CN105814092 B CN 105814092B
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- Prior art keywords
- methyl
- acid
- ester
- indicate
- sodium
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- 239000000203 mixture Substances 0.000 title claims abstract description 31
- 239000000463 material Substances 0.000 title abstract description 22
- 230000010148 water-pollination Effects 0.000 title abstract description 14
- -1 siloxanes Chemical class 0.000 claims abstract description 590
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 139
- 150000001875 compounds Chemical class 0.000 claims abstract description 111
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 94
- 125000000524 functional group Chemical group 0.000 claims abstract description 26
- 125000000129 anionic group Chemical group 0.000 claims abstract description 23
- 239000004094 surface-active agent Substances 0.000 claims abstract description 15
- 125000002091 cationic group Chemical group 0.000 claims abstract description 14
- 230000002209 hydrophobic effect Effects 0.000 claims abstract description 6
- 239000011347 resin Substances 0.000 claims abstract 3
- 229920005989 resin Polymers 0.000 claims abstract 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 774
- 239000002585 base Substances 0.000 claims description 312
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 189
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 133
- 150000001721 carbon Chemical group 0.000 claims description 69
- 239000000126 substance Substances 0.000 claims description 69
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 59
- 230000014509 gene expression Effects 0.000 claims description 46
- 125000004429 atom Chemical group 0.000 claims description 43
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 41
- 229910052783 alkali metal Inorganic materials 0.000 claims description 26
- 150000001340 alkali metals Chemical class 0.000 claims description 26
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 25
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 25
- 229910052701 rubidium Inorganic materials 0.000 claims description 22
- 125000000217 alkyl group Chemical group 0.000 claims description 21
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 19
- 229910019142 PO4 Inorganic materials 0.000 claims description 16
- 239000010452 phosphate Substances 0.000 claims description 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 15
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 14
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 13
- 235000019441 ethanol Nutrition 0.000 claims description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Natural products CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 11
- 125000006177 alkyl benzyl group Chemical group 0.000 claims description 10
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 claims description 10
- YZCKVEUIGOORGS-IGMARMGPSA-N Protium Chemical compound [1H] YZCKVEUIGOORGS-IGMARMGPSA-N 0.000 claims description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 7
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 claims description 7
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 5
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 4
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 claims 5
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 1
- 229910003827 NRaRb Inorganic materials 0.000 claims 1
- 238000009835 boiling Methods 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 229910052738 indium Inorganic materials 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 13
- 150000002148 esters Chemical class 0.000 description 407
- 229910052700 potassium Inorganic materials 0.000 description 168
- 239000011591 potassium Substances 0.000 description 168
- 229960003975 potassium Drugs 0.000 description 168
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 165
- 229910052708 sodium Inorganic materials 0.000 description 164
- 239000011734 sodium Substances 0.000 description 164
- 239000011575 calcium Substances 0.000 description 162
- 229910052791 calcium Inorganic materials 0.000 description 162
- 235000001465 calcium Nutrition 0.000 description 162
- 229960005069 calcium Drugs 0.000 description 162
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 161
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 161
- 229910052749 magnesium Inorganic materials 0.000 description 158
- 239000011777 magnesium Substances 0.000 description 158
- 235000001055 magnesium Nutrition 0.000 description 158
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 156
- 229910052744 lithium Inorganic materials 0.000 description 144
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 142
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 133
- FUZZWVXGSFPDMH-UHFFFAOYSA-N n-hexanoic acid Natural products CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 90
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 70
- 229940048053 acrylate Drugs 0.000 description 70
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 68
- CERQOIWHTDAKMF-UHFFFAOYSA-N alpha-methacrylic acid Natural products CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 66
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 52
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 50
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 48
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 44
- 239000001103 potassium chloride Substances 0.000 description 40
- 235000011164 potassium chloride Nutrition 0.000 description 40
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 39
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 36
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 36
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 35
- LVHBHZANLOWSRM-UHFFFAOYSA-N itaconic acid Chemical compound OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 33
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 32
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 31
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 31
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N Valeric acid Natural products CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 31
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 30
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 30
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 28
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 28
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 28
- 239000002253 acid Substances 0.000 description 28
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 28
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 28
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 27
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 26
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 25
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 25
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 24
- 241000255964 Pieridae Species 0.000 description 23
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 description 23
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 20
- 229960002446 octanoic acid Drugs 0.000 description 20
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 20
- 229910001413 alkali metal ion Inorganic materials 0.000 description 19
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 description 19
- 235000019260 propionic acid Nutrition 0.000 description 19
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 18
- 229940005605 valeric acid Drugs 0.000 description 18
- QFGCFKJIPBRJGM-UHFFFAOYSA-N 12-[(2-methylpropan-2-yl)oxy]-12-oxododecanoic acid Chemical compound CC(C)(C)OC(=O)CCCCCCCCCCC(O)=O QFGCFKJIPBRJGM-UHFFFAOYSA-N 0.000 description 17
- IAQRGUVFOMOMEM-UHFFFAOYSA-N but-2-ene Chemical group CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 17
- 125000000291 glutamic acid group Chemical group N[C@@H](CCC(O)=O)C(=O)* 0.000 description 15
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 15
- 125000005504 styryl group Chemical group 0.000 description 15
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 14
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 14
- 150000001336 alkenes Chemical class 0.000 description 14
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 description 14
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 13
- QOSMNYMQXIVWKY-UHFFFAOYSA-N Propyl levulinate Chemical compound CCCOC(=O)CCC(C)=O QOSMNYMQXIVWKY-UHFFFAOYSA-N 0.000 description 12
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 12
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 11
- 235000021317 phosphate Nutrition 0.000 description 11
- 239000001488 sodium phosphate Substances 0.000 description 11
- 235000011008 sodium phosphates Nutrition 0.000 description 11
- 229920002554 vinyl polymer Polymers 0.000 description 11
- OGVXMOUBEBDSLY-UHFFFAOYSA-N C(C=C)(=O)OC.C(CCCCC(=O)O)(=O)O Chemical compound C(C=C)(=O)OC.C(CCCCC(=O)O)(=O)O OGVXMOUBEBDSLY-UHFFFAOYSA-N 0.000 description 10
- TVIDDXQYHWJXFK-UHFFFAOYSA-N dodecanedioic acid Chemical compound OC(=O)CCCCCCCCCCC(O)=O TVIDDXQYHWJXFK-UHFFFAOYSA-N 0.000 description 10
- 239000004220 glutamic acid Substances 0.000 description 10
- UIIIBRHUICCMAI-UHFFFAOYSA-N prop-2-ene-1-sulfonic acid Chemical compound OS(=O)(=O)CC=C UIIIBRHUICCMAI-UHFFFAOYSA-N 0.000 description 10
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 description 10
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 10
- BDAGIHXWWSANSR-UHFFFAOYSA-N Formic acid Chemical compound OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 9
- DJOWTWWHMWQATC-KYHIUUMWSA-N Karpoxanthin Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1(O)C(C)(C)CC(O)CC1(C)O)C=CC=C(/C)C=CC2=C(C)CC(O)CC2(C)C DJOWTWWHMWQATC-KYHIUUMWSA-N 0.000 description 9
- BMRWNKZVCUKKSR-UHFFFAOYSA-N butane-1,2-diol Chemical class CCC(O)CO BMRWNKZVCUKKSR-UHFFFAOYSA-N 0.000 description 9
- OWBTYPJTUOEWEK-UHFFFAOYSA-N butane-2,3-diol Chemical class CC(O)C(C)O OWBTYPJTUOEWEK-UHFFFAOYSA-N 0.000 description 9
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 9
- 229940049920 malate Drugs 0.000 description 9
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 9
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- 235000011007 phosphoric acid Nutrition 0.000 description 9
- 229910000162 sodium phosphate Inorganic materials 0.000 description 9
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- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 8
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- 229910000388 diammonium phosphate Inorganic materials 0.000 description 8
- 235000019838 diammonium phosphate Nutrition 0.000 description 8
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 8
- 229930015698 phenylpropene Natural products 0.000 description 8
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- 159000000000 sodium salts Chemical class 0.000 description 8
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 8
- CREMOMAMRUYGQT-UHFFFAOYSA-N C(CCCCCCCCCCC(=O)O)(=O)O.C(C=C)(=O)OC Chemical compound C(CCCCCCCCCCC(=O)O)(=O)O.C(C=C)(=O)OC CREMOMAMRUYGQT-UHFFFAOYSA-N 0.000 description 7
- 241000534944 Thia Species 0.000 description 7
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
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- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical group CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 5
- MUWOTPLDXQSGQZ-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)propanoic acid Chemical compound OC(=O)C(C)OC(=O)C(C)=C MUWOTPLDXQSGQZ-UHFFFAOYSA-N 0.000 description 5
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- 239000004471 Glycine Substances 0.000 description 5
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 5
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- 235000013922 glutamic acid Nutrition 0.000 description 5
- 239000004137 magnesium phosphate Substances 0.000 description 5
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- 229960002261 magnesium phosphate Drugs 0.000 description 5
- 235000010994 magnesium phosphates Nutrition 0.000 description 5
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 5
- 150000003839 salts Chemical group 0.000 description 5
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- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 5
- GVGVTGDTIDAVMV-UHFFFAOYSA-N 2-but-2-enoyloxypropanoic acid Chemical class CC=CC(=O)OC(C(=O)O)C GVGVTGDTIDAVMV-UHFFFAOYSA-N 0.000 description 4
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- KHPJLRRQWDDJDW-UHFFFAOYSA-N anthracene;potassium Chemical compound [K].C1=CC=CC2=CC3=CC=CC=C3C=C21 KHPJLRRQWDDJDW-UHFFFAOYSA-N 0.000 description 1
- YZVHXQKDSLJLEH-UHFFFAOYSA-N azane 3-prop-1-en-2-ylbenzene-1,2-disulfonic acid Chemical compound N.CC(=C)c1cccc(c1S(O)(=O)=O)S(O)(=O)=O YZVHXQKDSLJLEH-UHFFFAOYSA-N 0.000 description 1
- NLVWBYNKMPGKRG-ODZAUARKSA-N azane;(z)-but-2-enedioic acid Chemical compound N.OC(=O)\C=C/C(O)=O NLVWBYNKMPGKRG-ODZAUARKSA-N 0.000 description 1
- OQTRPSFMBXCQIY-UHFFFAOYSA-N azane;2-methylidenebutanedioic acid Chemical compound N.OC(=O)CC(=C)C(O)=O OQTRPSFMBXCQIY-UHFFFAOYSA-N 0.000 description 1
- XZAVPVVTKGFNQK-UHFFFAOYSA-N azane;ethanesulfonic acid Chemical compound [NH4+].CCS([O-])(=O)=O XZAVPVVTKGFNQK-UHFFFAOYSA-N 0.000 description 1
- FBUKTRABNNLNSF-UHFFFAOYSA-N azanium 2-prop-1-en-2-ylbenzenesulfonate Chemical compound [NH4+].CC(=C)c1ccccc1S([O-])(=O)=O FBUKTRABNNLNSF-UHFFFAOYSA-N 0.000 description 1
- WZFOMMBSMSXIEP-UHFFFAOYSA-N azanium 4-prop-2-enoyloxypentane-1-sulfonate Chemical compound CC(CCCS(=O)(=O)[O-])OC(=O)C=C.[NH4+] WZFOMMBSMSXIEP-UHFFFAOYSA-N 0.000 description 1
- XDIJWRHVEDUFGP-UHFFFAOYSA-N azanium;2-phenylethenesulfonate Chemical compound [NH4+].[O-]S(=O)(=O)C=CC1=CC=CC=C1 XDIJWRHVEDUFGP-UHFFFAOYSA-N 0.000 description 1
- WWLOCCUNZXBJFR-UHFFFAOYSA-N azanium;benzenesulfonate Chemical compound [NH4+].[O-]S(=O)(=O)C1=CC=CC=C1 WWLOCCUNZXBJFR-UHFFFAOYSA-N 0.000 description 1
- SGIAKTJHCBPGOS-UHFFFAOYSA-N azanium;ethenesulfonate Chemical compound N.OS(=O)(=O)C=C SGIAKTJHCBPGOS-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- VNHHSBRJHXRDTE-UHFFFAOYSA-N benzenesulfonic acid;calcium Chemical compound [Ca].OS(=O)(=O)C1=CC=CC=C1 VNHHSBRJHXRDTE-UHFFFAOYSA-N 0.000 description 1
- IPLJXALXGKSNPT-UHFFFAOYSA-N benzenesulfonic acid;lithium Chemical compound [Li].OS(=O)(=O)C1=CC=CC=C1 IPLJXALXGKSNPT-UHFFFAOYSA-N 0.000 description 1
- FSTZWKIICVTWLA-UHFFFAOYSA-N benzenesulfonic acid;magnesium Chemical compound [Mg].OS(=O)(=O)C1=CC=CC=C1 FSTZWKIICVTWLA-UHFFFAOYSA-N 0.000 description 1
- VJAGHZLYXAKQID-UHFFFAOYSA-N benzenesulfonic acid;potassium Chemical compound [K].OS(=O)(=O)C1=CC=CC=C1 VJAGHZLYXAKQID-UHFFFAOYSA-N 0.000 description 1
- RYRCBNPVBZJZEV-UHFFFAOYSA-N benzenesulfonic acid;rubidium Chemical compound [Rb].OS(=O)(=O)C1=CC=CC=C1 RYRCBNPVBZJZEV-UHFFFAOYSA-N 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 235000019437 butane-1,3-diol Nutrition 0.000 description 1
- QDHFHIQKOVNCNC-UHFFFAOYSA-N butane-1-sulfonic acid Chemical compound CCCCS(O)(=O)=O QDHFHIQKOVNCNC-UHFFFAOYSA-N 0.000 description 1
- ATZRRRJPVCTDKR-UHFFFAOYSA-N butane-1-sulfonic acid;sodium Chemical compound [Na].CCCCS(O)(=O)=O ATZRRRJPVCTDKR-UHFFFAOYSA-N 0.000 description 1
- 229940034055 calcium aspartate Drugs 0.000 description 1
- 239000004227 calcium gluconate Substances 0.000 description 1
- 229960004494 calcium gluconate Drugs 0.000 description 1
- HDRTWMBOUSPQON-ODZAUARKSA-L calcium;(z)-but-2-enedioate Chemical compound [Ca+2].[O-]C(=O)\C=C/C([O-])=O HDRTWMBOUSPQON-ODZAUARKSA-L 0.000 description 1
- QMUKWBNHAAQQGV-UHFFFAOYSA-N calcium;2-methylidenebutanedioic acid Chemical compound [Ca].OC(=O)CC(=C)C(O)=O QMUKWBNHAAQQGV-UHFFFAOYSA-N 0.000 description 1
- LYMYOENPASUELF-UHFFFAOYSA-N calcium;2-methylprop-2-enoic acid Chemical compound [Ca].CC(=C)C(O)=O LYMYOENPASUELF-UHFFFAOYSA-N 0.000 description 1
- CNYFJCCVJNARLE-UHFFFAOYSA-L calcium;2-sulfanylacetic acid;2-sulfidoacetate Chemical compound [Ca+2].[O-]C(=O)CS.[O-]C(=O)CS CNYFJCCVJNARLE-UHFFFAOYSA-L 0.000 description 1
- AAESHKQBOSPIQC-UHFFFAOYSA-N calcium;ethenesulfonic acid Chemical compound [Ca].OS(=O)(=O)C=C AAESHKQBOSPIQC-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- SEGLCEQVOFDUPX-UHFFFAOYSA-N di-(2-ethylhexyl)phosphoric acid Chemical class CCCCC(CC)COP(O)(=O)OCC(CC)CCCC SEGLCEQVOFDUPX-UHFFFAOYSA-N 0.000 description 1
- UUIIVQKLPGPRKV-UHFFFAOYSA-N diazanium 2-phenylethene-1,1-disulfonate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)C(=Cc1ccccc1)S([O-])(=O)=O UUIIVQKLPGPRKV-UHFFFAOYSA-N 0.000 description 1
- CKKXWJDFFQPBQL-UAIGNFCESA-N diazanium;(z)-but-2-enedioate Chemical compound [NH4+].[NH4+].[O-]C(=O)\C=C/C([O-])=O CKKXWJDFFQPBQL-UAIGNFCESA-N 0.000 description 1
- FRKMZLXCWXPBOB-UHFFFAOYSA-N diazanium;2-methylidenebutanedioate Chemical compound [NH4+].[NH4+].[O-]C(=O)CC(=C)C([O-])=O FRKMZLXCWXPBOB-UHFFFAOYSA-N 0.000 description 1
- DGXRZJSPDXZJFG-UHFFFAOYSA-N docosanedioic acid Chemical class OC(=O)CCCCCCCCCCCCCCCCCCCCC(O)=O DGXRZJSPDXZJFG-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- CCIVGXIOQKPBKL-UHFFFAOYSA-N ethanesulfonic acid Chemical compound CCS(O)(=O)=O CCIVGXIOQKPBKL-UHFFFAOYSA-N 0.000 description 1
- DZQDWELKIPSRIS-UHFFFAOYSA-N ethanesulfonic acid;magnesium Chemical compound [Mg].CCS(O)(=O)=O DZQDWELKIPSRIS-UHFFFAOYSA-N 0.000 description 1
- UXCXDXQIWXBVNI-UHFFFAOYSA-N ethanesulfonic acid;potassium Chemical compound [K].CCS(O)(=O)=O UXCXDXQIWXBVNI-UHFFFAOYSA-N 0.000 description 1
- SDJHDRMYZQFJJO-UHFFFAOYSA-N ethanethioic s-acid;potassium Chemical compound [K].CC(S)=O SDJHDRMYZQFJJO-UHFFFAOYSA-N 0.000 description 1
- RGVQHDUEXIHFSS-UHFFFAOYSA-N ethenesulfonic acid;lithium Chemical compound [Li].OS(=O)(=O)C=C RGVQHDUEXIHFSS-UHFFFAOYSA-N 0.000 description 1
- ALVADSZPKQTQGQ-UHFFFAOYSA-N ethenesulfonic acid;magnesium Chemical compound [Mg].OS(=O)(=O)C=C ALVADSZPKQTQGQ-UHFFFAOYSA-N 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229940050410 gluconate Drugs 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 229940049906 glutamate Drugs 0.000 description 1
- 239000004247 glycine and its sodium salt Substances 0.000 description 1
- 238000005213 imbibition Methods 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- XIXADJRWDQXREU-UHFFFAOYSA-M lithium acetate Chemical compound [Li+].CC([O-])=O XIXADJRWDQXREU-UHFFFAOYSA-M 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 229960004254 lithium succinate Drugs 0.000 description 1
- PVUWSOGHWGLPPX-UHFFFAOYSA-N lithium;2-methylidenebutanedioic acid Chemical compound [Li].OC(=O)CC(=C)C(O)=O PVUWSOGHWGLPPX-UHFFFAOYSA-N 0.000 description 1
- OJUGTBALYKCJBW-UHFFFAOYSA-M lithium;bis(2-ethylhexyl) phosphate Chemical compound [Li+].CCCCC(CC)COP([O-])(=O)OCC(CC)CCCC OJUGTBALYKCJBW-UHFFFAOYSA-M 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 229940004916 magnesium glycinate Drugs 0.000 description 1
- HECDFHHTXWHSBH-UHFFFAOYSA-N magnesium;2-methylidenebutanedioic acid Chemical compound [Mg].OC(=O)CC(=C)C(O)=O HECDFHHTXWHSBH-UHFFFAOYSA-N 0.000 description 1
- PSEXPFNBJCCKPF-UHFFFAOYSA-N magnesium;methanesulfonic acid Chemical compound [Mg].CS(O)(=O)=O PSEXPFNBJCCKPF-UHFFFAOYSA-N 0.000 description 1
- 125000003099 maleoyl group Chemical group C(\C=C/C(=O)*)(=O)* 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 125000005394 methallyl group Chemical group 0.000 description 1
- DWNWZFAKFWMPTI-UHFFFAOYSA-N methanesulfonic acid;sodium Chemical compound [Na].CS(O)(=O)=O DWNWZFAKFWMPTI-UHFFFAOYSA-N 0.000 description 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Substances OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 1
- XJKPNRSAFFACRG-UHFFFAOYSA-N methylamino prop-2-enoate Chemical compound CNOC(=O)C=C XJKPNRSAFFACRG-UHFFFAOYSA-N 0.000 description 1
- YHWPRKXKQSKUSJ-UHFFFAOYSA-N methylazanium;prop-2-enoate Chemical compound [NH3+]C.[O-]C(=O)C=C YHWPRKXKQSKUSJ-UHFFFAOYSA-N 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 239000004238 monoammonium glutamate Substances 0.000 description 1
- AUCNMQYOQYTGPE-UHFFFAOYSA-N n-(hydroxymethyl)-n-methylprop-2-enamide Chemical compound OCN(C)C(=O)C=C AUCNMQYOQYTGPE-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OWVWGCVNBQLTDH-UHFFFAOYSA-N n-butyl-n-methylprop-2-enamide Chemical compound CCCCN(C)C(=O)C=C OWVWGCVNBQLTDH-UHFFFAOYSA-N 0.000 description 1
- ZOTWHNWBICCBPC-UHFFFAOYSA-N n-ethyl-n-methylprop-2-enamide Chemical compound CCN(C)C(=O)C=C ZOTWHNWBICCBPC-UHFFFAOYSA-N 0.000 description 1
- OFHYREWCAQPIQI-UHFFFAOYSA-N n-hexyl-n-methylprop-2-enamide Chemical compound CCCCCCN(C)C(=O)C=C OFHYREWCAQPIQI-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N n-propyl alcohol Natural products CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- URXNVXOMQQCBHS-UHFFFAOYSA-N naphthalene;sodium Chemical compound [Na].C1=CC=CC2=CC=CC=C21 URXNVXOMQQCBHS-UHFFFAOYSA-N 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- QFOYLCHPNNWUFY-UHFFFAOYSA-N phenanthrene-1-sulfonic acid Chemical compound C1=CC2=CC=CC=C2C2=C1C(S(=O)(=O)O)=CC=C2 QFOYLCHPNNWUFY-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 229940068988 potassium aspartate Drugs 0.000 description 1
- 239000004224 potassium gluconate Substances 0.000 description 1
- 229960003189 potassium gluconate Drugs 0.000 description 1
- 229910001414 potassium ion Inorganic materials 0.000 description 1
- QPMDWIOUHQWKHV-TYYBGVCCSA-M potassium;(e)-but-2-enedioate;hydron Chemical compound [H+].[K+].[O-]C(=O)\C=C\C([O-])=O QPMDWIOUHQWKHV-TYYBGVCCSA-M 0.000 description 1
- QKTYWKFUCQCNCV-UHFFFAOYSA-N potassium;2-prop-1-en-2-ylbenzenesulfonic acid Chemical compound [K].CC(=C)C1=CC=CC=C1S(O)(=O)=O QKTYWKFUCQCNCV-UHFFFAOYSA-N 0.000 description 1
- FWABLCJJBXRYBK-UHFFFAOYSA-N potassium;propane-1-sulfonic acid Chemical compound [K].CCCS(O)(=O)=O FWABLCJJBXRYBK-UHFFFAOYSA-N 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- ODBSOAATZFAZCB-UHFFFAOYSA-N prop-1-en-2-ylbenzene;sodium Chemical compound [Na].CC(=C)C1=CC=CC=C1 ODBSOAATZFAZCB-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 235000013849 propane Nutrition 0.000 description 1
- 229960004063 propylene glycol Drugs 0.000 description 1
- KOUKXHPPRFNWPP-UHFFFAOYSA-N pyrazine-2,5-dicarboxylic acid;hydrate Chemical compound O.OC(=O)C1=CN=C(C(O)=O)C=N1 KOUKXHPPRFNWPP-UHFFFAOYSA-N 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 229910001419 rubidium ion Inorganic materials 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 229940073490 sodium glutamate Drugs 0.000 description 1
- 229940029258 sodium glycinate Drugs 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 229940074404 sodium succinate Drugs 0.000 description 1
- GNBVPFITFYNRCN-UHFFFAOYSA-M sodium thioglycolate Chemical compound [Na+].[O-]C(=O)CS GNBVPFITFYNRCN-UHFFFAOYSA-M 0.000 description 1
- 229940046307 sodium thioglycolate Drugs 0.000 description 1
- SZHIIIPPJJXYRY-UHFFFAOYSA-M sodium;2-methylprop-2-ene-1-sulfonate Chemical compound [Na+].CC(=C)CS([O-])(=O)=O SZHIIIPPJJXYRY-UHFFFAOYSA-M 0.000 description 1
- MNCGMVDMOKPCSQ-UHFFFAOYSA-M sodium;2-phenylethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=CC1=CC=CC=C1 MNCGMVDMOKPCSQ-UHFFFAOYSA-M 0.000 description 1
- MZSDGDXXBZSFTG-UHFFFAOYSA-M sodium;benzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=CC=C1 MZSDGDXXBZSFTG-UHFFFAOYSA-M 0.000 description 1
- HIEHAIZHJZLEPQ-UHFFFAOYSA-M sodium;naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 HIEHAIZHJZLEPQ-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- KUCOHFSKRZZVRO-UHFFFAOYSA-N terephthalaldehyde Chemical compound O=CC1=CC=C(C=O)C=C1 KUCOHFSKRZZVRO-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/44—Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/24—Crosslinking, e.g. vulcanising, of macromolecules
- C08J3/245—Differential crosslinking of one polymer with one crosslinking type, e.g. surface crosslinking
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/043—Improving the adhesiveness of the coatings per se, e.g. forming primers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/054—Forming anti-misting or drip-proofing coatings
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/056—Forming hydrophilic coatings
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
- C09D4/06—Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09D159/00 - C09D187/00
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- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2369/00—Characterised by the use of polycarbonates; Derivatives of polycarbonates
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- C08J2435/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical, and containing at least one other carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Derivatives of such polymers
- C08J2435/02—Characterised by the use of homopolymers or copolymers of esters
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/06—Ethers; Acetals; Ketals; Ortho-esters
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
- C08K5/1545—Six-membered rings
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- C08K5/00—Use of organic ingredients
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- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/41—Compounds containing sulfur bound to oxygen
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- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/521—Esters of phosphoric acids, e.g. of H3PO4
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- Manufacturing & Machinery (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Paints Or Removers (AREA)
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Applications Claiming Priority (5)
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JP2013-256193 | 2013-12-11 | ||
JP2013256193 | 2013-12-11 | ||
JP2013256192 | 2013-12-11 | ||
JP2013-256192 | 2013-12-11 | ||
PCT/JP2014/082286 WO2015087810A1 (fr) | 2013-12-11 | 2014-12-05 | Composition pour un produit hydrophile durci |
Publications (2)
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CN105814092A CN105814092A (zh) | 2016-07-27 |
CN105814092B true CN105814092B (zh) | 2018-09-21 |
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CN201480067496.2A Expired - Fee Related CN105814092B (zh) | 2013-12-11 | 2014-12-05 | 亲水性固化物用组合物 |
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US (1) | US20180163056A1 (fr) |
EP (1) | EP3081578A4 (fr) |
JP (1) | JP6690943B2 (fr) |
KR (1) | KR101804083B1 (fr) |
CN (1) | CN105814092B (fr) |
PH (1) | PH12016501128A1 (fr) |
TW (1) | TWI658053B (fr) |
WO (1) | WO2015087810A1 (fr) |
Families Citing this family (12)
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JP5959764B2 (ja) * | 2014-05-19 | 2016-08-02 | 三井化学株式会社 | 親水性単層膜 |
KR20170012406A (ko) * | 2014-07-11 | 2017-02-02 | 미쓰이 가가쿠 가부시키가이샤 | 치과용 보철물 |
JPWO2018038271A1 (ja) * | 2016-08-26 | 2019-07-04 | 三井化学株式会社 | 反射防止性積層体 |
JP6731486B2 (ja) * | 2016-08-26 | 2020-07-29 | 三井化学株式会社 | 防曇性積層体 |
JP2019038140A (ja) * | 2017-08-23 | 2019-03-14 | 三井化学株式会社 | 防曇性フィルム、及び防曇性鏡 |
CN109676833B (zh) * | 2017-09-26 | 2022-01-18 | 夏普株式会社 | 合成高分子膜、其制造方法、杀菌方法、及光固化性树脂组合物 |
JP2019146538A (ja) * | 2018-02-28 | 2019-09-05 | 三井化学株式会社 | 水棲動植物用水槽および珪藻類の除去方法 |
WO2020013765A1 (fr) * | 2018-07-11 | 2020-01-16 | Structo Pte Ltd | Procédés et composition d'un modèle dentaire pour la fabrication d'appareils orthodontiques sans l'utilisation de séparateur |
JP7421281B2 (ja) * | 2019-06-10 | 2024-01-24 | 三井化学株式会社 | 易洗浄の衛生材料または生活用品、および微生物の除去方法 |
CN115677542A (zh) * | 2021-12-16 | 2023-02-03 | 上海银聪新材料科技有限公司 | 一种高闪点型长碳链酰胺丙基羟基磺基甜菜碱的合成方法 |
KR20230091472A (ko) * | 2021-12-16 | 2023-06-23 | 코오롱인더스트리 주식회사 | 광학 필름 및 이를 포함하는 표시장치 |
TWI804197B (zh) * | 2022-02-17 | 2023-06-01 | 紀騰縈 | 波哥特環保材料製造方法 |
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JP2007246835A (ja) * | 2006-03-17 | 2007-09-27 | Tokuyama Corp | 硬化性組成物 |
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2014
- 2014-12-05 US US15/102,454 patent/US20180163056A1/en not_active Abandoned
- 2014-12-05 EP EP14870377.0A patent/EP3081578A4/fr not_active Withdrawn
- 2014-12-05 CN CN201480067496.2A patent/CN105814092B/zh not_active Expired - Fee Related
- 2014-12-05 JP JP2015552425A patent/JP6690943B2/ja active Active
- 2014-12-05 WO PCT/JP2014/082286 patent/WO2015087810A1/fr active Application Filing
- 2014-12-05 KR KR1020167015025A patent/KR101804083B1/ko active IP Right Grant
- 2014-12-10 TW TW103142987A patent/TWI658053B/zh active
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2016
- 2016-06-10 PH PH12016501128A patent/PH12016501128A1/en unknown
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CN101309760A (zh) * | 2005-12-02 | 2008-11-19 | 三井化学株式会社 | 单层膜及由其构成的亲水性材料 |
JP2007246835A (ja) * | 2006-03-17 | 2007-09-27 | Tokuyama Corp | 硬化性組成物 |
CN101970553A (zh) * | 2008-03-21 | 2011-02-09 | 三井化学株式会社 | 亲水膜 |
CN101747690A (zh) * | 2008-11-28 | 2010-06-23 | 3M创新有限公司 | 防雾涂层组合物、防雾薄膜和制品 |
CN102666753A (zh) * | 2010-01-08 | 2012-09-12 | 日油株式会社 | 防雾涂料组合物 |
Also Published As
Publication number | Publication date |
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EP3081578A4 (fr) | 2017-06-21 |
KR20160084849A (ko) | 2016-07-14 |
JP6690943B2 (ja) | 2020-04-28 |
WO2015087810A1 (fr) | 2015-06-18 |
PH12016501128A1 (en) | 2016-07-18 |
TW201527325A (zh) | 2015-07-16 |
EP3081578A1 (fr) | 2016-10-19 |
TWI658053B (zh) | 2019-05-01 |
US20180163056A1 (en) | 2018-06-14 |
KR101804083B1 (ko) | 2017-12-01 |
JPWO2015087810A1 (ja) | 2017-03-16 |
CN105814092A (zh) | 2016-07-27 |
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